Schizophrenia:: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo

被引:439
作者
Do, KQ
Trabesinger, AH
Kirsten-Krüger, M
Lauer, CJ
Dydak, U
Hell, D
Holsboer, F
Boesiger, P
Cuénod, M
机构
[1] Univ Zurich, Brain Res Inst, CH-1008 Prilly, Switzerland
[2] Univ Lausanne, Ctr Res Psychiat Neurosci, CH-1008 Prilly, Switzerland
[3] Univ Zurich, Inst Biomed Engn, Zurich, Switzerland
[4] Swiss Fed Inst Technol, Zurich, Switzerland
[5] Psychiat Univ Hosp Zurich, Zurich, Switzerland
[6] Max Planck Inst Psychiat, Inst Clin, D-80804 Munich, Germany
关键词
dopamine; glutamate; human; magnetic resonance spectroscopy; oxidative stress;
D O I
10.1046/j.1460-9568.2000.00229.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Schizophrenia is a major psychiatric disease, which affects the centre of the personality, with severe problems of perception, cognition as well as affective and social behaviour. In cerebrospinal fluid of drug-free schizophrenic patients, a significant decrease in the level of total glutathione (GSH) by 27% (P < 0.05) was observed as compared to controls, in keeping with the reported reduced level of its metabolite gamma-glutamylglutamine. With a new non-invasive proton magnetic resonance spectroscopy methodology, GSH level in medial prefrontal cortex of schizophrenic patients was found to be 52% (P = 0.0012) lower than in controls. GSH plays a fundamental role in protecting cells from damage by reactive oxygen species generated among others by the metabolism of dopamine. A deficit in GSH would lead to degenerative processes in the surrounding of dopaminergic terminals resulting in loss of connectivity. GSH also potentiates the N-methyl-D-aspartate (NMDA) receptor response to glutamate, an effect presumably reduced by a GSH deficit, leading to a situation similar to the application of phencyclidine (PCP). Thus, a GSH hypothesis might integrate many established biological aspects of schizophrenia.
引用
收藏
页码:3721 / 3728
页数:8
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